| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Giuliana Grimaldi, Nordeyn Oulad Ben Taib, Mario Manto, Florian Bodranghie. Marked reduction of cerebellar deficits in upper limbs following transcranial cerebello-cerebral DC stimulation: tremor reduction and re-programming of the timing of antagonist commands. Frontiers in systems neuroscience. vol 8. 2014-02-13. PMID:24523678. |
cerebellar ataxias represent a very heterogeneous group of disabling disorders for which we lack effective symptomatic therapies in most cases. |
2014-02-13 |
2023-08-12 |
Not clear |
| Giuliana Grimaldi, Nordeyn Oulad Ben Taib, Mario Manto, Florian Bodranghie. Marked reduction of cerebellar deficits in upper limbs following transcranial cerebello-cerebral DC stimulation: tremor reduction and re-programming of the timing of antagonist commands. Frontiers in systems neuroscience. vol 8. 2014-02-13. PMID:24523678. |
our results indicate that tccdcs should be considered in the symptomatic management of upper limb motor deficits in cerebellar ataxias. |
2014-02-13 |
2023-08-12 |
Not clear |
| José Luiz Pedroso, Pedro Braga-Neto, Irapuá Ferreira Ricarte, Marcus Vinicius Cristino Albuquerque, Orlando Graziani Povoas Barsottin. Clinical spectrum of early onset cerebellar ataxia with retained tendon reflexes: an autosomal recessive ataxia not to be missed. Arquivos de neuro-psiquiatria. vol 71. issue 6. 2014-01-23. PMID:23828538. |
autosomal recessive cerebellar ataxias are a heterogeneous group of neurological disorders. |
2014-01-23 |
2023-08-12 |
Not clear |
| Ken Johkur. [Nystagmus the diagnosis of vertigo and dizziness]. Brain and nerve = Shinkei kenkyu no shinpo. vol 65. issue 9. 2014-01-09. PMID:24018742. |
vertigo/dizziness caused by disorders in the brainstem or upper cerebellum is usually associated with other neurological signs or symptoms, such as motor palsy, sensory deficit, dysarthria, ocular motor palsy, and limb ataxia. |
2014-01-09 |
2023-08-12 |
Not clear |
| Ken Johkur. [Nystagmus the diagnosis of vertigo and dizziness]. Brain and nerve = Shinkei kenkyu no shinpo. vol 65. issue 9. 2014-01-09. PMID:24018742. |
in contrast, vertigo/dizziness caused by disorders in the lower cerebellum is not associated with these signs or symptoms; however, truncal ataxia becomes apparent in a standing position. |
2014-01-09 |
2023-08-12 |
Not clear |
| Katsuya Araki, Tatsusada Okuno, Josephe Archie Honorat, Makoto Kinoshita, Masanori P Takahashi, Masao Mizuki, Kazuo Kitagawa, Hideki Mochizuk. [A case of chronic active Epstein-Barr virus infection associated with recurrent cerebellar ataxia and skin eruptions]. Rinsho shinkeigaku = Clinical neurology. vol 53. issue 2. 2013-12-17. PMID:23470892. |
five years later, at the age of 67, her ataxia relapsed concurrently with skin eruptions, whereas mri demonstrated progression of cerebellar atrophy. |
2013-12-17 |
2023-08-12 |
rat |
| Katsuya Araki, Tatsusada Okuno, Josephe Archie Honorat, Makoto Kinoshita, Masanori P Takahashi, Masao Mizuki, Kazuo Kitagawa, Hideki Mochizuk. [A case of chronic active Epstein-Barr virus infection associated with recurrent cerebellar ataxia and skin eruptions]. Rinsho shinkeigaku = Clinical neurology. vol 53. issue 2. 2013-12-17. PMID:23470892. |
furthermore, immunohistochemical analysis revealed a reactivity of the patient's serum and csf on rat cerebellum, suggesting an autoimmune pathomechanism for the ataxia. |
2013-12-17 |
2023-08-12 |
rat |
| Paulo Victor Sgobbi de Souza, Wladimir Bocca Vieira de Rezende Pinto, José Luiz Pedroso, Orlando Graziani Povoas Barsottin. Congenital ataxia due to cerebellar malformation presenting with unilateral hypoplasia. Arquivos de neuro-psiquiatria. vol 71. issue 3. 2013-12-17. PMID:23563724. |
congenital ataxia due to cerebellar malformation presenting with unilateral hypoplasia. |
2013-12-17 |
2023-08-12 |
Not clear |
| Vikas Kotaga. Acetazolamide-responsive ataxia. Seminars in neurology. vol 32. issue 5. 2013-12-17. PMID:23677664. |
acetazolamide-responsive ataxia represents a unique collection of genetically distinct episodic ataxia (ea) disorders associated with paroxysmal cerebellar symptoms many of which are responsive to medical treatment with acetazolamide, a carbonic anhydrase inhibitor. |
2013-12-17 |
2023-08-12 |
Not clear |
| Asif Iqbal, Kamlakar Tripathi, Madhukar Rai, Amit Nandan Dhar Dwived. Clinical and imaging perspective and unanswered questions in a case of metronidazole induced encephalopathy. Annals of Indian Academy of Neurology. vol 16. issue 4. 2013-12-16. PMID:24339581. |
the patient had ataxia and positive cerebellar signs. |
2013-12-16 |
2023-08-12 |
Not clear |
| Elisa J Cops, Maithili Sashindranath, Maria Daglas, Kieran M Short, Candida da Fonseca Pereira, Terence Y Pang, Roger H Lijnen, Ian M Smyth, Anthony J Hannan, Andre L Samson, Robert L Medcal. Tissue-type plasminogen activator is an extracellular mediator of Purkinje cell damage and altered gait. Experimental neurology. vol 249. 2013-12-09. PMID:23939410. |
a correlation between purkinje degeneration and excess cerebellar levels of tissue-type plasminogen activator (tpa) has been observed in multiple genetically-distinct models of ataxia. |
2013-12-09 |
2023-08-12 |
mouse |
| Marisa Brini, Tito Calì, Denis Ottolini, Ernesto Carafol. The plasma membrane calcium pump in health and disease. The FEBS journal. vol 280. issue 21. 2013-12-05. PMID:23413890. |
a cerebellar x-linked human ataxia has recently been found to be caused by a mutation in the calmodulin-binding domain of pmca3. |
2013-12-05 |
2023-08-12 |
mouse |
| Volga Tarlac, Louise Kelly, Nupur Nag, Judy Allen-Graham, Robert P Anderson, Elsdon Store. HLA-DR3-DQ2 mice do not develop ataxia in the presence of high titre anti-gliadin antibodies. Cerebellum (London, England). vol 12. issue 3. 2013-12-04. PMID:23086706. |
we aimed to determine whether mice transgenic for hla-dr3-dq2 and immunised with gliadin to achieve high titres of αgab would develop ataxia and/or cerebellar damage. |
2013-12-04 |
2023-08-12 |
mouse |
| Volga Tarlac, Louise Kelly, Nupur Nag, Judy Allen-Graham, Robert P Anderson, Elsdon Store. HLA-DR3-DQ2 mice do not develop ataxia in the presence of high titre anti-gliadin antibodies. Cerebellum (London, England). vol 12. issue 3. 2013-12-04. PMID:23086706. |
high levels of αgab are not sufficient to produce ataxia or cerebellar damage in hla-dr3-dq2 transgenic mice. |
2013-12-04 |
2023-08-12 |
mouse |
| Charlotte D C C van der Heijden, Mark Rijpkema, Alejandro Arias-Vásquez, Marina Hakobjan, Hans Scheffer, Guillen Fernandez, Barbara Franke, Bart P van de Warrenbur. Genetic variation in ataxia gene ATXN7 influences cerebellar grey matter volume in healthy adults. Cerebellum (London, England). vol 12. issue 3. 2013-12-04. PMID:23100044. |
genetic variation in ataxia gene atxn7 influences cerebellar grey matter volume in healthy adults. |
2013-12-04 |
2023-08-12 |
human |
| Charlotte D C C van der Heijden, Mark Rijpkema, Alejandro Arias-Vásquez, Marina Hakobjan, Hans Scheffer, Guillen Fernandez, Barbara Franke, Bart P van de Warrenbur. Genetic variation in ataxia gene ATXN7 influences cerebellar grey matter volume in healthy adults. Cerebellum (London, England). vol 12. issue 3. 2013-12-04. PMID:23100044. |
this finding may also imply that genes associated with cerebellar volume in healthy subjects are valid candidates for causing or modifying ataxia. |
2013-12-04 |
2023-08-12 |
human |
| M F Alexandre, S Rivaud-Péchoux, G Challe, A Durr, B Gaymar. Functional consequences of oculomotor disorders in hereditary cerebellar ataxias. Cerebellum (London, England). vol 12. issue 3. 2013-12-04. PMID:23239280. |
functional consequences of oculomotor disorders in hereditary cerebellar ataxias. |
2013-12-04 |
2023-08-12 |
human |
| Suman S Karanth, Anurag Gupta, Mukhyaprana Prabh. Pure cerebellitis due to scrub typhus: a unique case report. Tropical doctor. vol 43. issue 1. 2013-12-03. PMID:23550204. |
we report the case of a 24-year old indian man who presented with: high fever; drowsiness; an eschar and gross cerebellar dysfunction with horizontal gaze nystagmus; ataxic speech; and truncal ataxia. |
2013-12-03 |
2023-08-12 |
Not clear |
| Junko Sato, Satoshi Sasaki, Naoaki Yamada, Minoru Tsuchitan. Early morphological changes of hereditary cerebellar cortical abiotrophy in rabbits. The Journal of veterinary medical science. vol 75. issue 4. 2013-12-02. PMID:23182865. |
to estimate the onset time and incipient lesions associated with the cerebellar cortical abiotrophy of the cases, we mated the same pair again and examined early stages of the disease in f1 rabbit showing ataxia (pd 15), finding evidence that the ataxia is passed to subsequent generations via autosomal recessive inheritance. |
2013-12-02 |
2023-08-12 |
rabbit |
| Stacey L Reeber, Tom S Otis, Roy V Sillito. New roles for the cerebellum in health and disease. Frontiers in systems neuroscience. vol 7. 2013-12-02. PMID:24294192. |
serious damage to the cerebellum impairs this learning and results in a set of motor disturbances called ataxia. |
2013-12-02 |
2023-08-12 |
human |